Liquid crystalline peroxide compositions and methods for coloring and/or bleaching hair

ABSTRACT

An aqueous peroxide composition for coloring or lightening hair comprising (a) 1-99% of an aqueous phase containing (ii) 1-55% by weight of the total composition of water, (ii) 1-45% hydrogen peroxide, and (iii) a water soluble cosolvent; and (b) 0.1-60% of an oil phase; and (c) 1-65% of an organic, amphiphilic, surface active ingredient capable of interacting with the water phase and the oil phase to form lyotropic liquid crystals containing said water phase ingredients; a method for coloring or lightening hair using the peroxide composition, and a method for reducing the amount of time necessary to permanently color hair using the peroxide composition.

TECHNICAL FIELD

The invention is in the field of peroxide compositions for use in lightening or coloring hair, and methods for lightening or coloring hair using the composition.

BACKGROUND OF THE INVENTION

A large majority of women color their hair, either to cover gray or permanently change hair color. Permanent change in hair color may be obtained by oxidative dyes or bleaching. Oxidative hair dyes are widely used since they provide permanent color to hair, generally lasting from four to six weeks. Oxidative hair dyes are usually sold in the form of a two component kit. In one container is an aqueous alkaline composition in the liquid or crème form that contains oxidative dyes in addition to other ingredients. In the other container is a peroxide solution that contains an oxidizing agent, usually hydrogen peroxide. The two components are mixed immediately prior to use and applied to hair. The dye precursors in the lotion then penetrate the hair, and the oxidizing agent oxidizes the dye precursors to produce color in the hair, as well as lightening the melanin in the hair. The mixture is left on the hair for an appropriate period of time, generally 20 to 60 minutes, then rinsed off with water.

Most consumers complain that a hair color process that takes 20 to 60 minutes is too long. It is estimated that if oxidative dyeing and bleaching of hair were a 5 to 10 minute process, more consumers would be inclined to color their hair. Certain commercial products exist that advertise 5 to 10 minute color, but these systems only deposit temporary color on the surface of the hair and are not capable of permanently lightening hair, or causing a permanent color change to hair. Thus, the current commercial products have limited usefulness.

Accordingly, there is a need for providing compositions and processes for oxidative dyeing and/or bleaching of hair that enables permanent coloration of hair in 5 to 10 minutes. The coloring will include covering gray as well as providing permanent color change to the hair.

Liquid crystalline preparations are known for use in cosmetics and personal care products. Liquid crystals are a special phase of matter, in particular, the intermediate phase of matter that exists between a three dimensional ordered crystalline state and a disordered dissolved state. In a liquid crystal, some of the molecular order characteristics found in a solid phase are retained in the liquid state because of molecular orientation of molecules found within the composition. Many compounds are known to contribute to formation of liquid crystals; which have been widely used to encapsulate active ingredients, or act as delivery vehicles for drugs, cosmetics, fragrances, and the like.

For example, U.S. Pat. No. 5,688,831 teaches foundation makeup composition containing liquid crystals.

U.S. Pat. No. 5,696,074 teaches aqueous surfactant preparations containing liquid crystals. These aqueous surfactant compositions are used to prepare laundry and dishwashing detergents, or hair and body care preparations for cleansing or conditioning skin.

It has most unexpectedly been discovered that when peroxide compositions used in bleaching or oxidative dyeing of hair are in the liquid crystalline form, the amount of time necessary to lighten or color the hair is substantially reduced.

It is an object of the invention to provide a liquid crystalline peroxide composition for use in bleaching or oxidative dyeing of hair which is in a single phase.

It is another object of the invention to provide a peroxide composition for use in a five to ten minute process for bleaching or oxidative dyeing of hair.

It is another object of the invention to provide a method for oxidative dyeing and/or bleaching of hair in five to ten minutes.

It is another object of the invention to provide an oxidative hair dye or bleach composition mixed immediately prior to use, that is the liquid crystalline form.

It is another object of the invention to provide a method for reducing the amount of time necessary to permanently lighten or color hair in conventional products, by using liquid crystalline peroxide compositions.

It is another object of the invention to provide a method for permanently lightening or coloring hair with a liquid crystalline composition comprised of a mixture of liquid crystalline peroxide and an alkaline composition, wherein the presence of liquid crystals causes increased penetration of the active ingredients into the hair shaft, and thereby reduces the amount of time necessary to achieve lightening or permanent coloration of the hair.

SUMMARY OF THE INVENTION

The invention comprises an aqueous peroxide composition for coloring or lightening hair comprising:

(a) 1-99% of an aqueous phase containing:

(ii) 1-55% water,

(ii) 1-45% hydrogen peroxide, and

(iii) a water soluble cosolvent;

(b) 0.1-60% of an oil phase; and

(c) 1-65% of an organic, amphiphilic, surface active ingredient capable of interacting with the water phase and the oil phase to form lyotropic liquid crystals containing said water phase ingredients; wherein all percentages are percentages by weight of the total composition.

The invention also comprises a method for coloring or lightening hair comprising the steps of:

(a) combining, immediately prior to use,

(1) an aqueous alkaline composition comprising at least one interactive surfactant; and

(2) a peroxide composition for coloring or lightening hair comprising, by weight of the total composition:

(i) 1-99% of an aqueous phase containing:

(aa) 1-55% water,

(bb) 1-45% hydrogen peroxide, and

(cc) a water soluble cosolvent;

(ii) 0.1-60% of an oil phase; and

(iii) 1-65% of an organic, amphiphilic, surface active ingredient capable of interacting with the water phase and the oil phase to form lyotropic liquid crystals containing said water phase ingredients; wherein all percentages are percentages by weight of the total composition.

(b) applying said mixture of (1) and (2) to the hair to cause coloring or lightening of the hair.

The invention further comprises a method for reducing the amount of time required to lighten or permanently color hair (when compared to conventional products), comprising treating the hair with a mixture of a liquid crystalline peroxide composition and an aqueous alkaline composition containing an interactive surfactant.

DETAILED DESCRIPTION

All percentages mentioned herein are percentages by weight unless otherwise indicated. The term “liquid crystalline compositions” means compositions in accordance with the invention that contain liquid crystals as described herein. The term “liquid crystal” when used in accordance with the invention means nematic, lyotropic liquid crystals or smectic, lyotropic liquid crystals, or a combination of both. The term “lyotropic” means that the liquid crystalline system contains at least one polar solvent which may be water, a water soluble cosolvent, or the like. The term “nematic” means that the liquid crystal molecules are arranged in one dimensional order with random alignment in the second dimension. The term “smectic” means that the liquid crystal molecules are arranged in two dimensional sheets where the hydrogen bonding between the polar groups links the molecules laterally and cooperatively to form head-to-head and tail-to-tail bilayers. More preferably, the liquid crystals found in the compositions of the invention are in the rod or vesicle form and exhibit a lamellar form. The liquid crystalline state exists in, preferably, 20-99.99% by weight of the total peroxide composition. In addition, the peroxide composition is preferably a one phase composition, as opposed to a two phase emulsion composition having dispersed droplets in a continuous phase.

The term “coloring hair” in accordance with the method of the invention means permanently coloring hair with oxidative dyes, providing hair color that lasts about four to eight weeks.

The term “lightening hair” in accordance with the method of the invention, means permanent lightening of hair by a bleaching process, which causes permanent lightening of the melanin pigments found in the hair.

The term “single phase” means a composition that exists in one homogeneous phase or solution. Preferably, the single phase composition is clear or translucent.

I. THE PEROXIDE COMPOSITION

The peroxide composition comprises a water phase, an oil phase, and an organic, amphiphilic surface active ingredient capable of interacting with the water phase and the oil phase to form lyotropic liquid crystals having the aqueous phase ingredients contained therein. The interaction of the water phase, oil phase, and organic amphiphilic surface active ingredient preferably provides a single phase liquid crystalline composition that is clear or translucent.

A. The Aqueous Phase

The composition of the invention comprises 1-99%, preferably, 5-65%, more preferably 10-50% by weight of the total peroxide composition of an aqueous phase. The aqueous phase contains water, hydrogen peroxide, and one or more water soluble cosolvents, in addition to other desirable water soluble polar ingredients.

1. Water

The peroxide composition comprises, by total weight of the peroxide composition, about 1-55%, preferably 1-50%, more preferably 1-45% water.

2. Hydrogen Peroxide

The peroxide composition further comprises about 1-45%, preferably 1-40%, more preferably 1-35% by weight of the total peroxide composition of hydrogen peroxide.

3. Water Soluble Cosolvents

The peroxide composition comprises, 0.1-55%, preferably 0.5-50%, more preferably 1-45% by weight of the total peroxide composition of one or more water soluble cosolvents that interact with the other ingredients in the composition to form an environment suitable for the formation of liquid crystals. Suitable water soluble cosolvents include monohydric alcohols, glycols, polyols, and the like. Suitable monohydric alcohols include ethanol, propanol, and the like. Suitable glycols include propylene glycol, butylene glycol, ethylene glycol, and the like. Preferred is where the water soluble cosolvent is glycerol.

4. Other Ingredients

The water phase of the peroxide composition may additionally comprise one or more water soluble, polar ingredients that are compatible in the aqueous phase including monohydric alcohols, water soluble colorants, preservatives, and the like. These other water phase ingredients are, preferably, ingredients that enable the formation of a single phase composition.

B. The Oil Phase

The peroxide compositions of the invention comprise 0.1-60%, preferably 0.5-50%, more preferably 1-45% by weight of an oil phase. The term “oil phase” means at least one lipophilic ingredient that, either alone or in combination with other lipophilic ingredients, forms a liquid phase at room temperature, said liquid phase not being miscible with the water phase in the absence of the organic amphiphilic surface active agent. However, in the presence of the organic amphiphilic surface active agent, the lipophilic phase is capable of interacting with the water phase to form, preferably, a single phase composition.

The oil phase may be a volatile oil or a nonvolatile oil. The term “volatile” means an oil having a vapor pressure of 2 mm. of mercury or greater at 20° C. The term “nonvolatile” means an oil having a vapor pressure of less than 2 mm. of mercury at 20° C.

1. Volatile Oils

Suitable volatile oils for use in the composition include volatile paraffinic hydrocarbons generally have a viscosity of 0.5 to 10 centistokes at 25° C., and the like.

(a) Volatile Hydrocarbons

Suitable as the volatile oil are various straight or branched chain paraffinic hydrocarbons having 5 to 40 carbon atoms, more preferably 8-20 carbon atoms. Suitable hydrocarbons include pentane, hexane, heptane, decane, dodecane, tetradecane, tridecane, and C₈₋₂₀ isoparaffins as disclosed in U.S. Pat. Nos. 3,439,088 and 3,818,105, both of which are hereby incorporated by reference. Preferred volatile paraffinic hydrocarbons have a molecular weight of 70-225, preferably 160 to 190 and a boiling point range of 30 to 320, preferably 60-260 degrees C., and a viscosity of less than 10 cs. at 25 degrees C. Such paraffinic hydrocarbons are available from EXXON under the ISOPARS trademark, and from the Permethyl Corporation. Suitable C₁₂ isoparaffins, e.g. isododecane, are manufactured by Permethyl Corporation under the tradename Permethyl 99A Various C₁₆ isoparaffins commercially available, such as isohexadecane (having the tradename Permethyl R), are also suitable.

2. Nonvolatile Oils

A variety of nonvolatile oils are suitable for use in the peroxide compositions, including various nonvolatile organic oils. Suitable nonvolatile oils preferably have a viscosity of 10 to 1,000,000, preferably 20-500,000 centipoise at 25° C.

(a) Nonvolatile Organic Oils

(i) Esters

Examples of nonvolatile oils suitable for use in the compositions of the invention include esters formed by the reaction of carboxylic acid-containing compound with an aliphatic or aromatic alcohol. Preferably, such esters have the general formula RCO—OR′ wherein R and R′ are each independently a C₁₋₂₅, preferably a C₃₋₂₀ straight or branched chain alkyl, alkenyl or alkoxycarbonylalkyl or alkylcarbonyloxyalkyl. Examples of such esters include isopropyl myristate, isotridecyl isononanoate, isostearyl neopentanoate, tridecyl neopentanoate, cetyl octanoate, cetyl palmitate, cetyl ricinoleate, cetyl stearate, cetyl myristate, coco-dicaprylate/caprate, decyl isostearate, isodecyl oleate, isodecyl neopentanoate, isohexyl neopentanoate, octyl palmitate, dioctyl malate, tridecyl octanoate, myristyl myristate, octododecanol, and fatty alcohols such as oleyl alcohol, isocetyl alcohol, and the like, as well as the esters disclosed on pages 1558-1565 of the C.T.F.A. International Cosmetic Ingredient Dictionary and Handbook, Seventh Edition, 1997, which is hereby incorporated by reference.

Other esters include glyceryl esters of fatty acids, or triglycerides. Both vegetable and animal sources may be used. Examples of such oils include castor oil, lanolin oil, C₁₀₋₁₈ triglycerides, caprylic/capric/triglycerides, coconut oil, corn oil, cottonseed oil, linseed oil, mink oil, olive oil, palm oil, illipe butter, rapeseed oil, soybean oil, sunflower seed oil, walnut oil, and the like.

(ii) Hydrocarbons

Also suitable as the oil are nonvolatile hydrocarbons such as isoparaffins, hydrogenated polyisobutene, mineral oil, squalene, petrolatum, and so on.

(iii) Fatty Alcohols

Straight or branched chain fatty alcohols that are liquids at room temperature, having the formula R—OH wherein R is a straight or branched chain saturated or unsaturated alkyl having 6-30 carbon atoms, are also suitable oils. Such fatty alcohols include cetyl alcohol cetearyl alcohol, and the like.

(iv) Lanolin and Dervatives Thereof

Also suitable as the oil are various lanolin derivatives such as acetylated lanolin, acetylated lanolin alcohol, and so on.

In the preferred embodiment of the invention, the oil component comprises one or more nonvolatile organic oils which are esters, most particularly esters formed by the reaction of a short chain alcohol such as ethanol, isopropanol, and the like with a fatty acid having 10-22 carbon atoms. Most preferred is isopropyl myristate.

3. Other Ingredients

The peroxide composition may contain one or more additional ingredients that form part of the oil phase, provided those ingredients are lipophilic in character and are miscible with the other oil phase ingredients. Any additional oil phase ingredients should not interfere with the formation of liquid crystals in the composition, should interact with the other oil phase ingredients to facilitate formation of a single phase composition. Examples of such materials include waxes, preservatives, and the like.

C. Organic Amphiphilic Surface Active Material

The peroxide composition of the invention comprises 1-65%, preferably 3-60%, more preferably 5-55% by weight of an organic, amphiphilic, surface active material that is capable of interacting with the aqueous phase and the oil phase to form nematic or smectic lyotropic liquid crystals having the water phase ingredients contained therein. Preferably, the amphiphilic surface active material reacts with the aqueous phase and the oil phase to form a single phase composition which is most preferably clear or translucent. The term “amphiphilic” means that the surface active material contains both lipophilic and hydrophilic portions such that the hydrophilic portion of the molecule is attracted to, and orients with, the polar, aqueous phase ingredients in the composition, and the lipophilic portion of the molecule is attracted to, and orients with the nonpolar, oil phase of the peroxide composition. Examples of radicals that will confer hydrophilicity include hydroxy-polyethyleneoxy, hydroxyl, carboxylates, sulfonates, sulfates, phosphates, or amines. Examples of radicals that will confer lipophilicity are C₁₋₄₀ straight or branched chain alkyl, fluoro, aryl, aryloxy, C₁₋₄₀ hydrocarbyl acyl, hydroxypolypropyleneoxy, or mixtures thereof. The C₁₋₄₀ alkyl may be non-interrupted, or interruped by one or more oxygen atoms, a benzene ring, amides, esters, or other functional groups. In addition, the organic, amphiphilic, surface active agent should be capable of interacting with the aqueous and oil phases of the composition to form liquid crystals at temperatures ranging from 20 to 40° C., most preferably at 25° C., which is room temperature. Examples of suitable organic, amphiphilic, surface active agents include nonionic, amphoteric, cationic, and anionic surface active agents. The organic, amphiphilic, surface active agent may be a liquid, semi-solid, or solid at room temperature.

1. Nonionic Surface Active Agents

A variety of nonionic surface active agents are suitable for use as the organic, amphiphilic, surface active agents. Preferably, the nonionic surface active agents have an HLB (hydrophile/lipophile balance) of 12-20, more preferably 13-16. Examples of nonionic surfactants include:

(a) Alkoxylated Alcohols

Suitable alkoxylated alcohols include ethers formed from the reaction of an aliphatic, aromatic, or heterocyclic alcohol with an alkylene oxide, generally ethylene or propylene oxide. Preferably, the alcohol is an aliphatic alcohol, more preferably a fatty alcohol having 10-22 carbon atoms; and the alkylene oxide is ethylene oxide. Examples of preferred alkoxylated alcohols include steareth, ceteth, ceteareth, beheneth, and the like, having from 1 to 200 repeating ethylene oxide units, as well as PEG derivatives of fatty acids such as PEG dioleate, PEG distearate, PEG isostearate, and so on.

(b) Sorbitan Derivatives

Suitable sorbitan derivatives are esters or ethers or sorbitan, which is a heterocyclic ether formed by the dehydration of sorbitol. Sorbitan may be derivatized by ethoxylation and/or esterification of the hydroxyl groups. Suitable acids used for esterification include C1-30 acids, more preferably, fatty acids having 6-22 carbon atoms. Examples of suitable sorbitan derivatives include PEG derivatives of sorbitan wherein the number of repeating ethylene oxide units ranges from 2 to 200, such as PEG sorbitan beeswax, glyceryl/sorbitol/oleate/hydroxystearate, PEG sorbitan cocoate, PEG sorbitan diisostearate, PEG sorbitan isostearate, PEG sorbitan lanolate, PEG sorbitan laurate, PEG sorbitan oleate, PEG sorbitan palmitate, PEG sorbitan perisostearate, PEG sorbitan peroleate, PEG sorbitan stearate, PEG sorbitan tetraoleate, PEG sorbitan tetrastearate, PEg sorbitan triisostearate; Polysorbates such as Polysorbate 20-85, Polysorbtate 80 acetate; and sorbitan esters such as sorbitan caprylate, cocoate, diisostearate, dioleate, distearate, isostearate, laurate, oleate, olivate, palmitate, sesquiisostearate, sesquioleate, sesquistearate, stearate, triisostearate, trioleate and the like. Preferrred are Polysorbates, in particular Polysorbate 80.

(c) Glyceryl Ethers

Also suitable are linear or branched ethers of polyglycerol having the general formula:

R—(Gly)_(n)—OH

wherein n is 1-10 and R is a straight or branched, saturated or unsaturated alkyl having 6 to 30 carbon atoms, and Gly is the glycerol residue. Examples of suitable polyglyceryl derivatives include polyglyceryl decaoleates, polyglyceryl caprates, polyglyceryl diisostearates, polyglyceryl distearates, polyglyceryl isopalmitates, polyglyceryl laurates, and the like.

(d) Glyceryl Esters

Suitable glyceryl esters include alkoxylated glyceryl esters include synthetic or semi-synthetic glyceryl esters, e.g. fatty acid mono-, di-, and triglycerides which are natural fats or oils that have been modified, for example, by reaction with alkylene oxide units, preferably ethylene oxide units. Examples of such glyceryl esters include PEG glyceryl oleates, PEG glyceryl stearates and isostearates, PEG glyceryl laurates, PEG glyceryl tallowates, and so on. Preferred PEG glyceryl esters include those of the formula:

RC(O)OCH₂CH(OH)CH₂(OCH₂CH₂)_(n)OH

wherein n is 5-200 and RC(O)— is a hydrocarbylcarbonyl group wherein R is preferably an aliphatic radical having 7 to 19 carbon atoms.

Also suitable are glyceryl esters formed by the reaction of glycerol with one or more fatty acids. Examples of these glyceryl esters include glyceryl adipate, caprylate, cocoate, stearate, diisostearate, laurate, linoleate, and so on.

(e) Dialkyl Sulfoxides

Also suitable are long chain dialkyl sulfoxides containing one short chain alkyl or hydroxy alkyl radical of from about 1 to 3 carbon atoms and one long hydrophobic chain which may be an alkyl, alkenyl, hydroxyalkyl, or ketoalkyl radical containing from about 8 to 20 carbon atoms, from 0 to 10 ethylene oxide moieties, and 0 or 1 glyceryl moiety.

(f) Polyethylene Oxide Condensates of Alkyl Phenols

Suitable condensates include the condensation products of alkyl phenols having an alkyl group of 6 to 20 carbon atoms with ethylene oxide being present in amounts of about 10 to 60 moles of ethylene oxide per mole of alkyl phenol.

(g) Condensation Products of Ethylene Diamine

Examples of suitable condensation products of ethylene diamine include products of ethylene oxide with the reaction product of propylene oxide and ethylene diamine.

(h) Long Chain Tertiary Amine Oxides

Preferred long chain tertiary amine oxides include those corresponding to the general formula:

R₁R₂R₃NO

wherein R₁ contains an alkyl, alkenyl or monohydroxyalkyl radical ranging from about 8 to 18 carbon atoms in length, from 0 to about 10 ethylene oxide moieties, and from 0 to about 1 glyceryl moiety and R₂ and R₃ are each alkyl or monohydroxyalkyl groups containing from about 1 to about 3 carbon atoms.

(h) Long Chain Tertiary Phosphine Oxides

Suitable long chain tertiary phosphine oxides include those corresponding to the general formula:

RR₁R₂PO

wherein R contains an alkyl, alkenyl, or monohydroxyalkyl radical having 8 to 18 carbon atoms, from 0-10 ethylene oxide moieties and 0 or 1 glyceryl moiety, and R₂ and R₃ are each alkyl or monohydroxyalkyl group containing from about 1 to 3 carbon atoms.

(i) Polyhydroxyl Fatty Acid Amides

Examples of C₁₀₋₁₈ alkyl(C₁₋₆)polyhydroxy fatty acid amides such as C₁₂₋₁₈ methylglucamides, N-alkoxy polyhydroxy fatty acid amides, N-propyl through N-hexyl C₁₂₋₁₈ glucamides and so on.

(j) Alkyl Polysaccharides

Suitable nonionic surfactants are alkyl polysaccharides, or alkyl glycosides, disclosed in U.S. Pat. Nos. 5,716,418 and 5,756,079, both of which are hereby incorporated by reference. These alkylglycosides have the general formula:

R₁—O—(R₂O)_(t)—(G)_(n)—H

wherein R₁ is a linear or branched alkyl or alkenyl radical having 12 to 30 carbon atoms, R₂ is a C₂₋₄ alkylene, (G) is an anhydroglucose unit, t is a number between 0 and 10, preferably 0 to 4, and n is a number from about 1 to 15. Examples of such alkyl polysaccharides are octyl, nonydecyl, undecyldodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, and octadecyl, di-, tri-, tetra-, penta-, and hexaglucosides, galactosides, lactosides, glucoses, fructosides, fructoses, and so on. Certain polyglycosides having the above formula are sold by Henkel Corporation under the tradenamnes APG 300, APG 350, APG 500, APG 550, APG 625, or the tradename Planteren, e.g. Planteren 300, 600, 1200, 2000, and so on.

Particularly preferred nonionic surfactants for use in the peroxide compositions are sorbitan derivatives, in particular the Polysorbates.

2. Anionic Surfactants

Also suitable for use as the amphiphilic surface active material are one or more anionic surfactants.

(a) Alkyl Sulfates

Anionic surfactants include alkyl and alkyl ether sulfates generally having the formula ROSO₃M and RO(C₂H₄O)_(x)SO₃M wherein R is alkyl or alkenyl of from about 10 to 20 carbon atoms, x is 1 to about 10 and M is a water soluble cation such as ammonium, sodium, potassium, or triethanolamine cation.

Another type of anionic surfactant which may be used in the compositions of the invention are water soluble salts of organic, sulfuric acid reaction products of the general formula:

R₁—SO₃—M

wherein R₁ is chosen from the group consisting of a straight or branched chain, saturated aliphatic hydrocarbon radical having from about 8 to about 24 carbon atoms, preferably 12 to about 18 carbon atoms; and M is a cation. Examples of such anionic surfactants are salts of organic sulfuric acid reaction products of hydrocarbons such as n-paraffins having 8 to 24 carbon atoms, and a sulfonating agent, such as sulfur trioxide.

(b) Fatty Acids Esterified with Isethionic Acid

Also suitable as anionic surfactants are reaction products of fatty acids esterified with isethionic acid and neutralized with sodium hydroxide. The fatty acids may be derived from coconut oil, for example.

(c) Succinates or Succinimates

In addition, succinates and succinimates are suitable anionic surfactants. This class includes compounds such as disodium N-octadecylsulfosuccinate; tetrasodium N-(1,2-dicarboxyethyl)-N-octadecylsulfosuccinate; and esters of sodium sulfosuccinic acid e.g. the dihexyl ester of sodium sulfosuccinic acid, the dioctyl ester of sodium sulfosuccinic acid, and the like.

(d) Olefin Sulfonates

Other suitable anionic surfactants include olefin sulfonates having about 12 to 24 carbon atoms. The term “olefin sulfonate” means a compound that can be produced by sulfonation of an alpha olefin by means of uncomplexed sulfur trioxide, followed by neutralization of the acid reaction mixture in conditions such that any sultones which have been formed in the reaction are hydrolyzed to give the corresponding hydroxyalkanesulfonates. The alpha-olefin from which the olefin sulfonate is derived is a mono-olefin having about 12 to 24 carbon atoms, preferably about 14 to 16 carbon atoms.

Other classes of suitable anionic organic surfactants are the beta-alkoxy alkane sulfonates or water soluble soaps thereof such as the salts of C₁₀₋₂₀ fatty acids, for example coconut and tallow based soaps. Preferred salts are ammonium, potassium, and sodium salts.

(e) N-acyl Amino Acids

Still another class of anionic surfactants include N-acyl amino acid surfactants and salts thereof (alkali alkaline earth, and ammonium salts) having the formula:

wherein R₁ is a C₈₋₂₄ alkyl or alkenyl radical, preferably C₁₀₋₁₈; R₂ is H, C₁₋₄ alkyl, phenyl, or —CH₂COOM; R₃ is CX₂— or C₁₋₂ alkoxy, wherein each X independently is H or a C₁₋₆ alkyl or alkylester, n is from 1 to 4, and M is H or a salt forming cation as described above. Examples of such surfactants are the N-acyl sarcosinates, including lauroyl sarcosinate, myristoyl sarcosinate, cocoyl sarcosinate, and oleoyl sarcosinate, preferably in sodium or potassium forms.

Certain types of amphoteric, zwitterionic, or cationic surfactants may also be used as the amphiphilic surface active material. Descriptions of such surfactants are set forth in U.S. Pat. No. 5,843,193, which is hereby incorporated by reference in its entirety.

The peroxide composition is made by simply combining the ingredients and mixing well. Lyotropic liquid crystals will form upon mixing of the ingredients, and the liquid crystals will remain in the composition even after it is combined with the aqueous alkaline composition and applied to the hair.

II. THE AQUEOUS ALKALINE COMPOSITION

The aqueous alkaline composition comprises at least one interactive surfactant, and, when mixed with the peroxide composition, is capable of activating the peroxide composition so that it is will color and/or lighten hair. In addition, the aqueous alkaline composition is compatible with the peroxide composition such that when the two compositions are mixed immediately prior to use, the liquid crystals remain in the mixture and are available for deposition onto the hair. Preferably, the aqueous alkaline composition is in the form of an emulsion, which may be water in oil, or oil in water emulsion. When the aqueous alkaline emulsion composition is mixed with the single phase peroxide composition the liquid crystals remain in the mixture. After mixing, the mixture is applied to the hair and will lighten or bleach hair or both depending on whether the aqueous alkaline composition contains oxidative dyes. The aqueous alkaline composition preferably has a pH of 7.1 to 11, more preferably 7.5 to 9.5, most preferably 7.8 to 9.2. Preferably the aqueous alkaline composition comprises 10-95%, preferably 15-90%, more preferably 15-85% by weight of the total aqueous alkaline composition of water. If the aqueous alkaline composition contains one or more oxidative dyes, when combined with the peroxide composition, the mixture will oxidatively color hair. If the aqueous alkaline composition contains no oxidative dyes, it may simply act as an activator for the peroxide composition upon mixing, and when this mixture is applied to hair it will cause permanent lightening, or bleaching, of the hair. The aqueous alkaline composition preferably comprises one or more of the following ingredients:

A. Interactive Surfactant

The aqueous alkaline composition contains at least one interactive surfactant. The term “interactive surfactant” means any surfactant that is compatible with both the aqueous alkaline composition and the peroxide composition, such that when the peroxide composition and the aqueous alkaline composition are combined immediately prior to use, the mixture remains in the form of liquid crystals and are available for deposit and penetration into the hair. Suitable surfactants may be anionic, nonionic, amphoteric, or zwitterionic, provided they are compatible with the amphiphilic surfactant found in the peroxide composition such that when the peroxide composition and the oxidative dye compositions are combined immediately prior to use the liquid crystals remain stable in the mixture and are available for deposit and penetration into the hair.

Preferred interactive surfactants include the amphiphilic surfactants mentioned for use in the peroxide composition. In addition, amphoteric, zwitterionic, and cationic surfactants are also suitable provided they fulfill the requirements mentioned herein. Suggested ranges of interactive surfactant are 0.001-20%, preferably 0.01-15%, more preferably 0.05-10% by weight of the total aqueous alkaline composition.

1. Amphoteric Surfactants

Suitable amphoteric surfactants may be imidazolinium compounds having the general formula:

wherein R¹ is C₈₋₂₂ alkyl or alkenyl, preferably C₁₂₋₁₆; R² is hydrogen or CH₂CO₂, R³ is CH₂CH₂OH or CH₂CH₂OCH₂CHCOOM; R⁴ is hydrogen, CH₂CH₂OH, or CH₂CH₂OCH₂CH₂COOM, Z is CO₂M or CH₂CO₂M, n is 2 or 3, preferably 2, M is hydrogen or a cation such as an alkali metal, alkaline earth metal, ammonium, or alkanol ammonium. cation. Examples of such materials are marketed under the tradename MIRANOL, by Miranol, Inc.

Also suitable amphoteric surfactants are monocarboxylates or dicarboxylates such as cocoamphocarboxypropionate, cocoamphocarboxypropionic acid, cocoamphocarboxyglycinate, and cocoamphoacetate.

Other types of amphoteric surfactants include aminoalkanoates of the formula

R—NH(CH₂)COOM

or iminodialkanoates of the formula:

R—N[(CH₂)_(m)COOM]₂

and mixtures thereof; wherein n and m are 1 to 4, R is C₈₋₂₂ alkyl or alkenyl, and M is hydrogen, alkali metal, alkaline earth metal, ammonium or alkanolammonium. Examples of such amphoteric surfactants include n-alkylaminopropionates and n-alkyliminodipropionates, which are sold under the trade name MIRATAINE by Miranol, Inc. or DERIPHAT by Henkel, for example N-lauryl-beta-amino propionic acid, N-lauryl-beta-imino-dipropionic acid, or mixtures thereof.

2. Zwitterionic Surfactants

Zwitterionic surfactants are also suitable for use in the aqueous alkaline compositions of the invention. The general formula for such surfactants is:

wherein R₂ contains an alkyl, alkenyl or hydroxy alkyl radical of from about 8 to about 18 carbon atoms, from 0 to about 10 ethylene oxide moieties and 0 or 1 glyceryl moiety; Y is selected from the group consisting of nitrogen, phosphorus, and sulfur atoms; R₃ is an alkyl or monohydroxyalkyl group containing about 1 to 3 carbon atoms; X is 1 when Y is a sulfur atom, and 2 when Y is a nitrogen or phosphorus atom; R₄ is an alkylene or hydroxyalkylene of from about 1 to about 4 carbon atoms, and Z is a radical selected from the group consisting of carboxylate, sulfonate, sulfate, phosphonate, and phosphate groups.

Zwitterionics include betaines, for example higher alkyl betaines such as coco dimethyl carboxymethyl betaine, lauryl dimethyl carboxymethyl betaine, lauryl dimethyl alpha-carboxyethyl betaine, cetyl dimethyl carboxymethyl betaine, lauryl bis-(2-hydroxyethyl)carboxymethyl betaine, stearyl bis-(2-hydroxypropyl)carboxymethyl betaine, oleyl dimethyl gamma-carboxylethyl betaine, and mixtures thereof. Also suitable are sulfo- and amido- betaines such as coco dimethyl sulfopropyl betaine, stearyl dimethyl sulfopropyl betaine, and the like.

3. Cationic Surfactants

The aqueous alkaline composition may comprise 0.01-15%, preferably 0.05-10%, preferably 0.10-8% of a cationic surfactant which is, preferably a quaternary ammonium salt or the salt of a fatty amine. Quaternary ammonium salts have the formula:

wherein R₁ is hydrogen, an aliphatic group of 1 to 22 carbon atoms, or aromatic, aryl, or alkaryl group having 12 to 22 carbon atoms; R₂ is an aliphatic group having 1-22 carbon atoms; R₃ and R₄ are each alkyl groups of from 1 to 3 carbon atoms, and X is an anion selected from halogen, acetate, phosphate, nitrate and methyl sulfate radicals. The aliphatic groups may contain, in addition to carbon and hydrogen atoms, ether linkages as well as amido groups. Suitable quaternary ammonium compounds may be mono-long chain alkyl, di-long chain alkyl, tri-long chain alkyl, and the like. Examples of such quaternary ammonium salts include behenalkonium chloride, behentrimonium chloride, behentrimonium methosulfate, benzalkonium chloride, benzethonium chloride, benzyl triethyl ammonium chloride, cetalkonium chloride, cetrimonium chloride, cetrimonium bromide, cetrimonium methosulfate, cetrimonium tosylate, cetylpyridinium chloride, dibehenyl/diarachidyl dimonium chloride, dibehenyldimonium chloride, dibehenyldimonium methosulfate, dicapryl/dicaprylyl dimonium chloride, dicetyldimonium chloride, and mixtures thereof.

Other quaternary ammonium salts useful as the cationic conditioning agent are compounds of the general formula:

wherein R₁ is an aliphatic group having 16 to 22 carbon atoms, R₂, R₃, R₄, R₅, and R₆ are the same or different and are selected from H and alkyls having 1 to 4 carbon atoms and X is an anion as above defined.

Also, quaternary imidazolinium salts having the following general formula are also suitable:

wherein R₅ is hydrogen or a C₁₋₄ alkyl; R is a C₁₋₄ alkyl; R₇ is a C₈₋₂₂ alkyl; and R₈ is hydrogen, or a C₁₋₂₂ alkyl; and X is an anion as defined above.

Also suitable are salts of fatty primary, secondary, or tertiary amines, wherein the substituted groups have 12 to 22 carbon atoms. Examples of such amines include dimethyl stearamine, dimethyl soyamine, stearylamine, myristylamine, tridecylamine, ethyl stearamine, and so on.

B. Oxidative Dyes

Where the aqueous alkaline composition is in the form of an oxidative dye, the composition will comprise at least one primary intermediate and, optionally, at least one coupler for the formation of oxidation dyes. Examples of suitable oxidative dyes and oxidative dye compositions include those set forth in U.S. Pat. No. 5,143,193, which is hereby incorporated by reference.

1. Primary Intermediates and Couplers

If the aqueous alkaline composition is in the form of an oxidative hair dye composition the composition contains 0.0001-20%, preferably 0.001-15%, more preferably 0.01-10% (combined weight) of at least one primary intermediate and, optionally, at least one coupler for the formation of oxidation dyes. Preferably, the oxidative dye composition will contain one or more of both a primary intermediate and coupler, and if so, the range of primary intermediate will be about 0.0001-5% by weight and the range of coupler will be about 0.0001-5% by weight. Primary intermediates and couplers are well known hair coloring ingredients, and include ortho or para substituted aminophenols or phenylenediamines, such as para-phenylenediamines of the formula:

wherein R₁ and R₂ are each independently hydrogen, C₁₋₆ alkyl, or C₁₋₆ alkyl substituted with one or more hydroxy, methoxy, methylsulphonylamino, aminocarbonyl, furfuryl, unsubstituted phenyl, or amino substituted phenyl groups; R₃ and R₆ are each independently hydrogen, C₁₋₆ alkyl C₁₋₆ alkoxy, halogen, or C₁₋₆ alkyl substituted with one or more hydroxyl groups; and R₄ and R₅ are each independently hydrogen, C₁₋₆ lower alkoxy, C₁₋₆ lower alkyl, or halogen. Examples of suitable primary intermediates are para-aminophenol, para-hydroquinone, ortho-hydroquinone, ortho-phenylenediamines, ortho-diphenols, para-phenylenediamine, 2-methyl-1,4-diaminobenzene, 2,6-dimethyl-1,4-diaminobenzene, 2,5-dimethyl-1,4-diaminobenzene, 2,3-dimethyl-1,4-diaminobenzene, 2-chloro-1,4-diaminobenzene, 2-methoxy-1,4-diaminobenzene, 1-phenylamino-4-aminobenzene, 1-dimethylamino-4-aminobenzene, 1-diethylamino-4-aminobenzene, 1-bis(beta-hydroxyethyl)amino-4-aminobenzene, 1-methoxyethylamino-4-aminobenzene, 2-hydroxymethyl-1,4-diaminobenzene, 2-hydroxyethyl-1,4-diaminobenzene, 2-isopropyl-1,4-diaminobenzene, 1-hydroxypropylamino-4-aminobenzene, 2,6-dimethyl-3-methoxy-1,4-diaminobenzene, and derivatives thereof.

Preferred primary intermediates are p-phenylenediamine, p-aminophenol, o-aminophenol, N,N-bis(2-hydroxyethyl)-p-phenylenediamine, 2,5-diaminotoluene, their salts and mixtures thereof.

Suitable couplers include, for example, those having the general formula:

wherein R₁ is unsubstituted hydroxy or amino, or hydroxy or amino substituted with one or more C₁₋₆ hydroxyalkyl groups, R₃ and R₅ are each independently hydrogen, hydroxy, amino, or amino substituted with C₁₋₆ alkyl, C₁₋₆ alkoxy, or C₁₋₆ hydroxyalkyl group; and R₂, R₄, and R₆ are each independently hydrogen, C₁₋₆ alkoxy, C₁₋₆ alkoxy, C₁₋₆ hydroxyalkyl or C₁₋₆ alkyl, or R₃ and R₄ together may form a methylenedioxy group. Examples of such compounds include meta-derivatives such as phenols, resorcinols, meta-aminophenols, meta-phenylenediamines, and the like, which may be unsubstituted, or substituted on the amino group or benzene ring with alkyl, hydroxyalkyl, aminoalkyl groups, and the like. Suitable couplers include 3,4-methylenedioxyphenol, 3,4-methylenedioxy-1-[(beta-hydroxyethyl)amino]benzene, 1-methoxy-2-amino-4-[(beta-hydroxyethyl)amino]benzene, 1-hydroxy-3-(dimethylamino)benzene, 6-methyl-1-hydroxy-3[(beta-hydroxyethyl)amino]benzene, 2,4-dichloro-1-hydroxy-3-aminobenzene, 1-hydroxy-3-(diethylamino)benzene, 1-hydroxy-2-methyl-3-aminobenzene, 2-chloro-6-methyl-1-hydroxy-3-aminobenzene, 1,3-diaminobenzene, 6-methoxy-1,3-diaminobenzene, 6-hydroxyethyloxy-1,3-diaminobenzene, 6-methoxy-5-ethyl-1,3-diaminobenzene, 6-ethyloxy-1,3-diaminobenzene, 1-bis(beta-hydroxyethyl)amino-3-aminobenzene, 2-methyl-1,3-diaminobenzene, 6-methoxy-1-amino-[(beta-hydroxyethyl)amino]-benzene, 6-(beta-aminoethyloxy)-1,3-diaminobenzene, 6-(beta-hydroxyethyloxy)-1-amino-3-(methylamino)benzene, 6-carboxymethyloxy-1,3-diaminobenzene, 6-ethyloxy-1-bis(beta-hydroxyethyl)amino-3-aminobenzene, 6-hydroxyethyl-1,3-diaminobenzene, 1-hydroxy-2-isopropyl-5-methylaminobenzene, 1,3-dihydroxybenzene, 2-chloro-1,3-dihydroxybenzene, 2-methyl-1,3-dihydroxybenzene, 4-chloro-1,3-dihydroxybenzene, 5,6-dichloro-2-methyl-1,3-dihydroxybenzene, 1-hydroxy-3-amino-benzene, 1-hydroxy-3-(carbamoylmethylamino)benzene, 6-hydroxybenzomorpholine, 4-methyl-6-dihydroxypyridine, 2,6-dihydroxypyridine, 2,6-diaminopyridine, 6-aminobenzomorpholine, 1-phenyl-3-methyl-5-pyrazolone, 1-hydroxynaphthalene, 1,7-dihydroxynaphthalene, 1,5-dihydroxynaphthalene, and mixtures thereof.

Preferred couplers include resorcinol, 1-naphthol, 5-amino-o-cresol, resorcinol, 2-methylresorcinol, m-aminophenol, m-phenylenediamine, 1-phenyl-3-methyl-pyrazol-5-one, their salts, or mixtures thereof.

C. Other Ingredients

The aqueous alkaline composition may contain one or more additional ingredients such as those set forth below:

1. Water Soluble Cosolvents

The aqueous alkaline composition may contain one or more water soluble cosolvents, and if so, suggested ranges are 0.001-20%, preferably 0.01-15%, more preferably 0.1-10% by weight of the total oxidative dye composition is suggested. Suitable water soluble cosolvents include glycols such as polyethylene glycol, propylene glycol, butylene glycol, glycerol, and the like.

2. Preservatives

The aqueous alkaline composition may also contain 0.0001-7%, preferably 0.001-5%, more preferably 0.005-3% preservatives. Suitable preservatives include methyl, ethyl, and propyl paraben, DMDM hydantoin, DEDM hydantoin, benzyl alcohol, the the like.

3. Chelating Agents

The aqueous alkaline composition may also contain 0.0001-5%, preferably 0.0005-3%, more preferably 0.001-2% of one or more chelating agents which are capable of complexing with and inactivating metallic ions in order to prevent their adverse effects on the stability or effects of the composition. In particular, the chelating agent in the developer will chelate the metal ions found in the water and prevent these ions from interfering with the reaction between the dye molecules and the oxidizing agent. Suitable chelating agents include EDTA and calcium, sodium, or potassium derivatives thereof, HEDTA, sodium citrate, TEA-EDTA, and so on.

4. pH Adjusters

It may also be desireable to add small amounts of acids or bases to adjust the pH of the aqueous alkaline composition to the desired pH range of 7.1 to 11. Suitable acids include hydrochloric acid, phosphoric acid, citric acid, and the like. Suitable bases include sodium hydroxide, potassium hydroxide, and the like.

5. Protein Derivatives

In addition, conditioning agents such as protein derivatives may be added to the aqueous alkaline composition. Generally about 0.001-10%, preferably 0.005-8%, more preferably 0.01-5% by weight of the total composition of protein derivatives is suggested. Examples of protein derivatives are hydrolyzed wheat protein, hydrolyzed wheat protein/wheat oligosaccharides, hydrolyzed marine collagen, wheat amino acids, PVP/hydrolyzed wheat protein copolymer (which is a copolymer of polyvinylpyrrolidone and hydrolyzed wheat protein).

6. Plant Extracts

It may also be desireable to include various plant extracts in the aqueous alkaline composition for extra conditioning and humectancy. Suggested ranges are 0.001-10%, preferably 0.005-8%, more preferably 0.01-5% by weight of the total composition. A preferred plant extract is seaweed extract.

7. Oils

The aqueous alkaline composition may contain one or more oils, and may be in the form of a water in oil or oil in water emulsion. Suggested ranges of oil are 0.1-40%, preferably 0.5-30%, more preferably 1-25% by weight of the total oxidative dye composition. Suitable oils are the esters and other oils mentioned for use in the peroxide composition.

8. Cationic Conditioning Polymers

The aqueous alkaline composition may contain one or more cationic conditioning polymers. Suggested ranges are 0.01-20%, preferably 0.05-15%, more preferably 0.1-10% by weight of the total aqueous alkaline composition. Examples of cationic conditioning polymers include:

(a) Quaternary derivatives of cellulose ethers such as polymers sold under the tradename JR-125, JR400, JR-30M. Preferred is Polyquaternium 10, which is a polymeric quaternary ammonium salt of hydroxyethyl cellulose reacted with a trimethyl ammonium subsituted epoxide.

(b) Copolymers of vinylpyrrolidone having monomer units of the formula:

wherein

R¹ is hydrogen or methyl, preferably methyl;

y is 0 or 1, preferably 1

R² is O or NH, preferably NH;

R³ is C_(x)H_(2x) where x is 2 to 18, or —CH₂—CHOH—CH₂—, preferably C_(x)H_(2x) where x is 2;

R⁴ is methyl, ethyl, phenyl, or C₁₋₄ substituted phenyl, preferably methyl; and

R⁵ is methyl or ethyl, preferably methyl; and m and n are each independently 1-10,000.

Preferred are compounds of the above formula wherein y is 1, R² is NH, R³ is CH₂CH₂, R⁴ is methyl, and R⁵ is methyl. Such compounds are known by the CTFA designation Polyquaternium 28.

(c) Homopolymer of dimethyldiallylammonium chloride, or copolymer of dimethyldiallylammonium chloride and acrylamide. Such compounds are sold under the tradename MERQUAT™ by Merck.

(d) Homopolymers or copolymers derived from acrylic methacrylic acid wherein the monomer units are selected from the group consisting of acrylamide, methylacrylamide, diacetone-acrylamide, acrylamide or methacrylamide substituted on the nitrogen by lower alkyl, alkyl esters of acrylic acid and methacrylic acid, vinylpyrrolidone, and vinyl esters.

Examples of cationic polymers that can be used in the compositions of the invention are the cationic polymers disclosed in U.S. Pat. Nos. 5,240,450 and 5,573,709, which are hereby incorporated by reference.

Preferred aqueous alkaline compositions for oxidative dyeing of hair comprise:

0.0001-20% (combined weight) of at least one primary intermediate and, optionally, at least one coupler for the formation of oxidation dyes,

0.001-20% of an interactive surfactant,

10-95% water.

Preferred aqueous alkaline compositions for bleaching of hair comprise:

0.001-20% of an interactive surfactant,

10-95% water, and

0.001-20% water soluble cosolvent.

If desired, both compositions may contain one or more of the ingredients mentioned above.

III. THE METHOD

The invention comprises a method for oxidative dyeing of hair comprising the steps of:

(a) combining, immediately prior to use,

(1) an aqueous oxidative dye composition comprising at least one primary intermediate and, optionally, at least one coupler for the formation of oxidation dyes and an interactive surfactant; and

(2) a peroxide composition for oxidative dyeing of hair comprising, by weight of the total composition:

(i) 1-99% of a water phase containing:

(aa) 1-55% water,

(bb) 1-45% hydrogen peroxide, and

(cc) a water soluble cosolvent;

(ii) 0.1-60% of an oil phase; and

(iii) 1-65% of an organic, amphiphilic, surface active ingredient capable of interacting with the water phase and the oil phase to form lyotropic liquid crystals containing said water phase ingredients; all percentages being by weight of the total peroxide composition;

(b) applying said mixture of (1) and (2) to the hair for an amount of time, preferably 5 to 10 minutes, to cause permanent coloration of hair.

In the method of the invention, about 1 to 5 parts of the peroxide composition is mixed with about 1 to 5 parts of the oxidative dye composition immediately prior to application on the hair. The mixture is applied to the hair and allowed to remain for the desired time period, which is preferably 5 to 10 minutes. If desired, the mixture can be left on the hair longer if, for example, the hair is very resistant to dye. Thereafter, the mixture is rinsed from the hair with water until clean. If desired, a hair conditioner may be applied to the hair.

The invention also comprises a method for bleaching hair comprising the steps of:

(a) combining, immediately prior to use,

(1) an aqueous alkaline compostion comprising at least one interactive surfactant; and

(2) a peroxide composition comprising, by weight of the total composition:

(i) 1-99% of a water phase containing:

(aa) 1-55% water,

(bb) 1-45% hydrogen peroxide, and

(cc) a water soluble cosolvent;

(ii) 0.1-60% of an oil phase; and

(iii) 1-65% of an organic, amphiphilic, surface active ingredient capable of interacting with the water phase and the oil phase to form lyotropic liquid crystals containing said water phase ingredients; all percentages being by weight of the total peroxide composition;

(b) applying said mixture of (1) and (2) to the hair for an amount of time, preferably 5 to 10 minutes, to cause lightening or bleaching of the hair.

In the bleaching method of the invention, about 1 to 5 parts of the peroxide composition is mixed with about 1 to 5 parts of the aqueous alkaline composition immediately prior to application on the hair. The mixture is applied to the hair and allowed to remain for the desired time period, which is preferably 5 to 10 minutes. If desired, the mixture can be left on the hair longer if, for example, the hair is very resistant to bleach. Thereafter, the mixture is rinsed from the hair with water until clean. If desired, a hair conditioner may be applied to the hair.

The invention further comprises a method for reducing the amount of time required to permanently color hair, comprising treating the hair with a mixture of a liquid crystalline peroxide composition and an aqueous alkaline composition containing at least one interactive surfactant.

The presence of liquid crystal particles in the mixture causes increased penetration of the oxidizing agent into the hair shaft, and thereby decreasing the amount of time necessary to achieve full coloration or lightening of the hair.

The compositions and methods of the invention provide permanent coloration or lightening of hair in as little as five to ten minutes. The coloring and/or lightening is permanent, which means that it lasts from about four to eight weeks.

The invention will be further described in connection with the following examples, which are set forth for the purposes of illustration only.

EXAMPLE 1

A peroxide composition in the liquid crystalline form was prepared according to the following formula:

w/w % Water  2.00 Hydrogen peroxide (35% aqueous solution) 18.00 Tween 80* 30.00 Isopropyl myristate 30.00 Glycerol 20.00 *Polysorbate 80: oleate esters of sorbitol and sorbitol anhydrides condensed with about 20 moles of ethylene oxide.

The composition was prepared by combining all of the ingredients and mixing well. The compositions were stored in an airtight plastic container.

EXAMPLE 2

A composition for oxidative dyeing of hair was made as follows:

w/w % Ammonium lauryl sulfate (anionic surfactant) 2.00 Propylene glycol (water soluble cosolvent) 4.00 Ethoxydiglycol (solvent) 2.00 Monoethanolamine (pH adjuster) 5.00 Seaweed extract (conditioner) 0.80 EDTA (chelating agent) 0.80 Isoascorbic acid (antioxidant) 0.20 Sodium sulfite (reducing agent) 0.50 Primary intermediates and couplers (dye) 5.00 Oleic acid (soap) 12.50  Cetearyl alcohol (opacifier) 4.00 Emulsifying wax (emulsifier) 2.00 Oleth-20 (nonionic surfactant) 1.00 Steareth-21 (nonionic surfactant) 0.70 Meadowfoam seed oil (oil) 0.75 Oleyl alcohol (oil) 0.40 Polyquaternium 10 (cationic conditioning agent) 0.20 Polyquaternium 28 (cationic conditioning agent) 0.50 Mica/titanium dioxide (colorant) 0.30 Hydrolyzed wheat protein (conditioner) 1.00 Cibafast W liquid* (UV absorber) 1.00 Fragrance 0.75 Ammonium hydroxide (pH adjuster) 5.00 Wheat amino acids (conditioner) 1.00 Water QS *sodium isobutyl benzotriazole sulfonate, Ciba Geigy

The composition was made by first dissolving the first eight ingredients in water. The primary intermediates and couplers were then added with heat to dissolve. The remaining ingredients, except for the ammonium hydroxide, wheat amino acids, and fragrance were mixed separately and added after the primary intermediates and couplers. The remaining water, ammonium hydroxide, hydrolyzed wheat protein, wheat amino acids, and fragrance were finally added to the mixture.

EXAMPLE 3

About 1.5 parts of the peroxide composition of Example 1 was mixed with 1 part of the oxidative hair dye composition of Example 2 and applied to hair. The composition was left on the hair for five minutes, and then rinsed out with water. The resulting hair was completely colored.

EXAMPLE 4

An aqueous alkaline composition suitable for mixing with the peroxide composition to form a hair bleach was prepared as follows:

w/w % Erythrobic acid 0.20 Sodium sulfite 0.50 Propylene glycol 4.00 Ethoxydiglycol 2.00 Tetrasodium EDTA (38% aqueous solution) 0.80 Ethanolamine 5.00 Hypnea musciformis extract/gellidiela acerosa/ 0.80 extract, sargassum filipendula extract/sorbitol Sodium benzotriazole sulfonate/buteth-3/propane 1.00 tricarboxylic acid Ammonium lauryl sulfate (28% aqueous solution) 2.00 Oleic acid 12.50  Cetearyl alcohol 4.00 Emulsifying wax 2.00 Oleth-20 1.00 Steareth-21 0.70 Meadowfoam seed oil 0.75 Oleyl alcohol 0.40 Polyquaternium-10 0.20 Polyquaternium-28 0.50 Mica/titanium dioxide (67:33) 0.30 Hydrolyzed wheat protein 1.00 Wheat amino acids 1.00 Fragrance 0.75 Ammonium hydroxide (27.5% aqueous solution) 5.00 Water QS

The composition was prepared by combining all of the ingredients and mixing well.

EXAMPLE 5

About 1.5 parts of the peroxide composition of Example 1 was mixed with 1 part of the Example 4 composition. The mixture was applied to hair and allowed to remain for 10 minutes, then rinsed out with water. The resulting hair was lightened at least three shades.

While the invention has been described in connection with the preferred embodiment, it is not intended to limit the scope of the invention to the particular form set forth but, on the contrary, it is intended to cover such alternatives, modifications, and equivalents as may be included within the spirit and scope of the invention as defined by the appended claims. 

We claim:
 1. An aqueous single phase peroxide composition for coloring or lightening hair comprising: (a) 1-99% of an aqueous phase containing: (ii) 1-55% by weight of the total composition of water, (ii) 1-45% hydrogen peroxide, and (iii) a water soluble cosolvent; (b) 0.1-60% of an oil phase; and (c) 1-65% of an organic, amphiphilic, surface active ingredient capable of interacting with the water phase and the oil phase to form lyotropic liquid crystals containing said water phase ingredients; all percentages being by weight of the total peroxide composition.
 2. The composition of claim 1 wherein the water soluble cosolvent comprises one or more sugars, glycols, or polyols.
 3. The composition of claim 2 wherein the water soluble cosolvent is a polyol.
 4. The composition of claim 1 wherein the oil phase comprises a nonvolatile oil.
 5. The composition of claim 4 wherein the nonvolatile oil comprises an organic oil.
 6. The composition of claim 5 wherein the nonvolatile oil comprises an organic oil which is an ester, hydrocarbon, fatty alcohol, lanolin, or mixtures thereof.
 7. The composition of claim 6 wherein the nonvolatile oil comprises an ester of the formula RCO—OR′ wherein R and R′ are each independently a C₁₋₂₅, preferably a C₄₋₂₀ straight or branched chain alkyl, alkenyl or alkoxycarbonylalkyl or alkylcarbonyloxyalkyl.
 8. The composition of claim 1 wherein the organic, amphiphilic, surface active ingredient is a nonionic, anionic, amphoteric, zwitterionic, or cationic surfactant, or mixtures thereof.
 9. The composition of claim 8 wherein the organic amphiphilic surface active ingredient comprises a nonionic or anionic surfactant, or mixtures thereof.
 10. The composition of claim 9 wherein the nonionic surfactant is an alkoxylated alcohol, sorbitan derivative, glyceryl ether, glyceryl ester, alkyl polysaccharde, or mixtures thereof.
 11. A method for coloring or lightening hair comprising the steps of: (a) combining, immediately prior to use, (1) an aqueous alkaline composition comprising at least one interactive surfactant; and (2) a single phase peroxide composition comprising, by weight of the total composition: (i) 1-99% of a water phase containing: (aa) 1-55% water, (bb) 1-45% hydrogen peroxide, and (cc) a water soluble cosolvent; (ii) 0.1-60% of an oil phase; and (iii) 1-65% of an organic, amphiphilic, surface active ingredient (b) applying said mixture of (1) and (2) to the hair to cause lightening or coloring of the hair.
 12. The method of claim 11 wherein the mixture is left on the hair for five to ten minutes.
 13. The method of claim 11 wherein the aqueous alkaline composition is an oxidative dye composition further comprising at least one primary intermediate for the formation of oxidation dyes.
 14. The method of claim 13 wherein the oxidative dye composition contains 0.001-5% by weight of the total composition of at least one primary intermediate and at least one coupler for the formation of oxidation dyes.
 15. The method of claim 11 wherein the mixture of the aqueous alkaline composition and the peroxide composition forms a composition which bleaches the hair.
 16. The method of claim 10 wherein the interactive surfactant comprises an anionic surfactant.
 17. The method of claim 10 wherein the aqueous alkaline composition is in the form of an emulsion.
 18. The method of claim 10 wherein the aqueous alkaline composition has a pH of 7.1 to
 11. 19. A method for reducing the amount of time required to permanently color hair, comprising treating the hair with a mixture of a liquid crystalline peroxide composition and an aqueous alkaline composition containing an interactive surfactant. 